ClearanceBrief
510(k) K834436 ยท FMI Needle, Hypodermic, Single Lumen

CHEMONUCLEOLYSIS NEEDLE

ApplicantUniversal Medical Instrument Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 15, 1984
ReceivedDec 19, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834436

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.